Food safety inspections are being scaled back and the public was not notified after an investigation into E. coli ...

Carroll County will start using LifeVac, an over-the-counter anti-choking device not approved by the FDA, in schools and first responder kits despite claims that it does not work.

Guidance language now reflects anticipation of FDA decision upon post-market study plan approval, compared to prior uncertainty about regulatory timing. The focus on US commercialization and sales ...

The Escherichia coli bacteria that ravaged Colton's kidneys was a genetic match to the strain that killed one person and ...

In the EU, GOHIBIC (vilobelimab) has been granted marketing authorization under exceptional circumstances for the treatment ...

Omeros faces critical liquidity challenges, with limited cash runway and rising dilution risks. Its cash runway is ...

BeOne Medicines Ltd. (NASDAQ: ONC; HKEX: 06160; SSE: 688235), a global oncology company formerly known as BeiGene, Ltd., ...

A new law approved by a wide margin and signed by Gov. Katie Hobbs will curb how those state-regulated marijuana ...

Despite hiring a commercial chief and sponsoring disease awareness efforts last year, Savara will have to wait a while longer ...

Abbott today announced the U.S. Food and Drug Administration (FDA) has approved the company's Tendynetm transcatheter mitral valve replacement (TMVR) system to treat people with mitral valve disease.

"We view the totality of the data in the NAUTILUS study as a meaningful catalyst that adds to the growing body of evidence and momentum in our business,” said Joel Becker, Chief Executive Officer.